Cellular mechanisms of complex I-associated pathology

被引:37
作者
Abramov, Andrey Y. [1 ]
Angelova, Plamena R. [1 ,2 ]
机构
[1] UCL, Dept Clin & Movement Neurosci, Inst Neurol, Queen Sq, London WC1N 3BG, England
[2] Sechenov First Moscow State Med Univ, Dept Pathophysiol, Moscow 119048, Russia
关键词
MITOCHONDRIAL CA2+; SEIZURE ACTIVITY; DEFICIENCY; DYSFUNCTION; MUTATIONS; FIBROBLASTS; SUBUNIT; GENE; TOXICITY; DELETION;
D O I
10.1042/BST20191042
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mitochondria control vitally important functions in cells, including energy production, cell signalling and regulation of cell death. Considering this, any alteration in mitochondrial metabolism would lead to cellular dysfunction and the development of a disease. A large proportion of disorders associated with mitochondria are induced by mutations or chemical inhibition of the mitochondrial complex I - the entry point to the electron transport chain. Subunits of the enzyme NADH: ubiquinone oxidoreductase, are encoded by both nuclear and mitochondrial DNA and mutations in these genes lead to cardio and muscular pathologies and diseases of the central nervous system. Despite such a clear involvement of complex I deficiency in numerous disorders, the molecular and cellular mechanisms leading to the development of pathology are not very clear. In this review, we summarise how lack of activity of complex I could differentially change mitochondrial and cellular functions and how these changes could lead to a pathology, following discrete routes.
引用
收藏
页码:1963 / 1969
页数:7
相关论文
共 63 条
  • [1] Mitochondrial Ca2+ in neurodegenerative disorders
    Abeti, Rosella
    Abramov, Andrey Y.
    [J]. PHARMACOLOGICAL RESEARCH, 2015, 99 : 377 - 381
  • [2] Interaction of misfolded proteins and mitochondria in neurodegenerative disorders
    Abramov, Andrey Y.
    Berezhnov, Alexey V.
    Fedotova, Evgeniya I.
    Zinchenko, Valery P.
    Dolgacheva, Ludmila P.
    [J]. BIOCHEMICAL SOCIETY TRANSACTIONS, 2017, 45 : 1025 - 1033
  • [3] Mechanism of neurodegeneration of neurons with mitochondrial DNA mutations
    Abramov, Andrey Y.
    Smulders-Srinivasan, Tora K.
    Kirby, Denise M.
    Acin-Perez, Rebeca
    Antonio Enriquez, Jose
    Lightowlers, Robert N.
    Duchen, Michael R.
    Turnbull, Douglass M.
    [J]. BRAIN, 2010, 133 : 797 - 807
  • [4] Role of mitochondrial ROS in the brain: from physiology to neurodegeneration
    Angelova, Plamena R.
    Abramov, Andrey Y.
    [J]. FEBS LETTERS, 2018, 592 (05) : 692 - 702
  • [5] Mitochondrial dysfunction in Parkinsonian mesenchymal stem cells impairs differentiation
    Angelova, Plamena R.
    Barilani, Mario
    Lovejoy, Christopher
    Dossena, Marta
    Vigano, Mariele
    Seresini, Agostino
    Piga, Daniela
    Gandhi, Sonia
    Pezzoli, Gianni
    Abramov, Andrey Y.
    Lazzari, Lorenza
    [J]. REDOX BIOLOGY, 2018, 14 : 474 - 484
  • [6] Functional role of mitochondrial reactive oxygen species in physiology
    Angelova, Plamena R.
    Abramov, Andrey Y.
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2016, 100 : 81 - 85
  • [7] Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome
    Bénit, P
    Slama, A
    Cartault, F
    Giurgea, I
    Chretien, D
    Lebon, S
    Marsac, C
    Munnich, A
    Rötig, A
    Rustin, P
    [J]. JOURNAL OF MEDICAL GENETICS, 2004, 41 (01) : 14 - 17
  • [8] Large-scale deletion and point mutations of the nuclear NDUFV1 and NDUFS1 genes in mitochondrial complex I deficiency
    Bénit, P
    Chretien, D
    Kadhom, N
    de Lonlay-Debeney, P
    Cormier-Daire, V
    Cabral, A
    Peudenier, S
    Rustin, P
    Munnich, A
    Rötig, A
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (06) : 1344 - 1352
  • [9] Neuronal and astrocyte dysfunction diverges from embryonic fibroblasts in the Ndufs4 fky fky mouse
    Bird, Matthew J.
    Wijeyeratne, Xiaonan W.
    Komen, Jasper C.
    Laskowski, Adrienne
    Ryan, Michael T.
    Thorburn, David R.
    Frazier, Ann E.
    [J]. BIOSCIENCE REPORTS, 2014, 34 : 701 - 715
  • [10] Clinical and molecular findings in children with complex I deficiency
    Bugiani, M
    Invernizzi, F
    Alberio, S
    Briem, E
    Lamantea, E
    Carrara, F
    Moroni, I
    Farina, L
    Spada, M
    Donati, MA
    Uziel, G
    Zeviani, M
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2004, 1659 (2-3): : 136 - 147